Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114012716 1.000 0.080 6 31466589 non coding transcript exon variant G/A snv 1
rs114042950 1.000 0.080 6 32699098 intergenic variant A/G snv 1
rs114050967 1.000 0.080 6 31537703 intron variant A/G snv 1
rs114388793 1.000 0.080 6 32699566 intergenic variant A/T snv 1
rs114771815 1.000 0.080 6 31484059 intron variant T/C snv 1
rs115146037 1.000 0.080 6 31466554 non coding transcript exon variant A/T snv 1
rs115902351 1.000 0.080 6 31466844 non coding transcript exon variant A/G snv 1
rs116088953 1.000 0.080 6 31475005 intron variant G/A snv 1
rs116662199 1.000 0.080 6 31481199 non coding transcript exon variant C/A snv 1
rs3130614 1.000 0.080 6 31508681 intron variant T/A snv 7.3E-02 1
rs6599390 1.000 0.080 4 962259 intron variant A/G snv 0.69 1
rs9267488 1.000 0.080 6 31546470 splice region variant A/G snv 8.1E-02 9.9E-02 1
rs13101828 0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs35677470 0.807 0.160 3 58197909 missense variant G/A;C snv 4.8E-02; 4.0E-06 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs10954214 0.851 0.160 7 128949579 3 prime UTR variant C/T snv 0.64 4
rs11085725 0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs112846137 0.851 0.160 3 160595133 intergenic variant G/T snv 5.3E-02 4
rs1217393 0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs13389408 0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02 4
rs193107685 0.851 0.160 7 74123572 downstream gene variant T/C snv 1.0E-02 4
rs2422345 0.851 0.160 1 173368608 upstream gene variant G/A snv 0.63 4
rs3129843 0.827 0.160 6 32427949 intergenic variant A/G snv 6.3E-02 4
rs4958880 0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs5754467 0.851 0.160 22 21630805 upstream gene variant A/G;T snv 4